About the IWMF

The International Waldenstrom’s Macroglobulinemia Foundation (IWMF)
We are a non-profit organization supports everyone affected by Waldenstrom's macroglobulinemia while advancing the search for a cure. Since 1999, the IWMF has funded more than $18 million in global WM research. We are a patient-founded and patient-driven, nonprofit organization that is dedicated to a simple but compelling vision and mission.


Our Vision
A World without WM (Waldenstrom's macroglobulinemia).

Our Mission
Supporting and educate everyone affected by Waldenstrom's macroglobulinemia (WM) while advancing the search for a cure.

Learn more about the IWMF at iwmf.com. Reach out to the IWMF office: 941-927-4963 or email office@iwmf.com with any questions you might have.

 

Meeting the Needs of the WM Community

In these uncertain times, the IWMF is pivoting to provide virtual programs to connect with attendees across the world. These immersive events information and tools necessary for making decisions about your Waldenstrom’s macroglobulinemia care. Networking is an important part of live events, so look for opportunities to virtually connect and engage with other attendees. When we cannot meet in-person virtual events are the next best thing!

 

Welcome to the IWMF Community

Although WM is a rare disease, the very first thing you should know is that you are not alone. Whether you are a patient, a caregiver, a family member or a friend of someone with WM, you have come to the right place. While having WM can at times be overwhelming and you may feel like you are on an emotional roller coaster, please know that the IWMF is here for you and your loved ones to help you understand WM and to offer education and support.

Join IWMF Community